FDA.reportPublic FDA data

FDA label ffd4eecd-51ba-4ff3-9828-f29b2b4cce81

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
aa189b1a-ce65-4896-a14d-7e8a8546a624
SPL ID
ffd4eecd-51ba-4ff3-9828-f29b2b4cce81
Version
1
Effective date
2021-03-31
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:33:40

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings • Be careful not to get in your eyes. • If it gets into your eyes, immediately wash it off with clean water several times. • Wear appropriate gloves during the procedure. • Do not eat. • Keep out of reach of children. • Store in a cool place away from direct sunlight. • Recommended for single use only. • For professional use only. • Follow the recommendations. • After use, if skin irritation such as rash or itching persists, stop use and consult a doctor or pharmacist

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.